Evidence map›Paper›PMID 15146062›Full record

ArticleMolecular biology of the cell2004

Cell cycle-dependent regulation of a human DNA helicase that localizes in DNA damage foci.

Jinming Gu, Xiaobo Xia, Peijun Yan, Hanjian Liu, Vladimir N Podust, Albert B Reynolds, Ellen Fanning

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
0.4field-weighted citation impact, top 41% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

41 citing papers in PubMed, 71 citations in OpenAlex.

  1. Trial
  2. A Constellation of Fluorescent Biosensors to Illuminate the Galaxy of Protein Kinases.Chembiochem : a European journal of chemical biology · 2026
    Review
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  6. Rare SNP in theNAR molecular medicine · 2025
    Article
  7. Article
  8. A concise guide to fluorescent cell cycle reporters for live-cell imaging.Frontiers in cell and developmental biology · 2025
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. SCFCell death & disease · 2020
    Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Jinming GuDepartment of Biological Sciences, Vanderbilt University, Nashville, Tennessee 37235, USA.
Xiaobo Xia
Peijun Yan
Hanjian Liu
Vladimir N Podust
Albert B Reynolds
Ellen Fanning
Vanderbilt University · US

Funding

CONTROL OF SIMIAN VIRUS 40 AND CELLULAR DNA REPLICATIONR01GM052948 · NIGMS · VANDERBILT UNIVERSITY · PI FRIEDMAN, KATHERINE LOUISE · 1995 to 2013
$6.1M
PL20 AND CELL CELL ADHESIONR01CA055724 · NCI · VANDERBILT UNIVERSITY · PI REYNOLDS, ALBERT B · 1997 to 2010
$2.9M
SUBSTRATES OF P60SRC PROTEIN TYROSINE KINASER29CA055724 · NCI · VANDERBILT UNIVERSITY · PI REYNOLDS, ALBERT B · 1992 to 1996
–
NCI NIH HHS CA-55724NCI NIH HHS CA-69485NCI NIH HHS R01 CA055724NIGMS NIH HHS GM-52948NIGMS NIH HHS R01 GM052948
6 · The paper itself

Abstract

Mutational studies of human DNA helicase B (HDHB) have suggested that its activity is critical for the G1/S transition of the cell cycle, but the nature of its role remains unknown. In this study, we show that during G1, ectopically expressed HDHB localizes in nuclear foci induced by DNA damaging agents and that this focal pattern requires active HDHB. During S and G2/M, HDHB localizes primarily in the cytoplasm. A carboxy-terminal domain from HDHB confers cell cycle-dependent localization, but not the focal pattern, to a reporter protein. A cluster of potential cyclin-dependent kinase phosphorylation sites in this domain was modified at the G1/S transition and maintained through G2/M of the cell cycle in vivo, coincident with nuclear export of HDHB. Serine 967 of HDHB was the major site phosphorylated in vivo and in vitro by cyclin-dependent kinases. Mutational analysis demonstrated that phosphorylation of serine 967 is crucial in regulating the subcellular localization of ectopically expressed HDHB. We propose that the helicase of HDHB operates primarily during G1 to process endogenous DNA damage before the G1/S transition, and it is largely sequestered in the cytoplasm during S/G2.

Indexed as

Cell CycleDNA DamageAmino Acid MotifsAmino Acid SequenceCamptothecinCDC2-CDC28 KinasesCyclin-Dependent Kinase 2DNADNA HelicasesDNA Mutational AnalysisG1 PhaseHumansIntracellular SpaceMitomycinMolecular Sequence DataPhosphorylationCamptothecinCDC2-CDC28 KinasesCDK2 protein, humanCyclin-Dependent Kinase 2DNADNA HelicasesMitomycinSerine

Identifiers

PMID15146062
PMCPMC452586
OpenAlexW2118182552

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.